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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268764Generated: October 30, 2026

Tetrabutylammonium Fluoride → N-(1H-Indol-4-yl)-2-methylamino-N-phenyl-acetamide

https://huagongshe.com/reaction/268764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-Methylamino-N-phenyl-N-(1-triisopropylsilanyl-1H-indol-4-yl)-acetamideHCID 59831839—
SolventTetrahydrofuranHCID 8028—
ProductN-(1H-Indol-4-yl)-2-methylamino-N-phenyl-acetamideHCID 59831661—

Reaction Steps

To a room temperature solution of 2-methylamino-N-phenyl-N-(1-triisopropylsilanyl-1H-indol-4-yl)-acetamide XXIII in THF (5 ml) was added tetrabutylammonium fluoride (TBAF) (149 mg, 0.566 mmol). The mixture was stirred for 18 hours and then partitioned between EtOAc and a saturated solution of NaHCO3. The aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated. The crude N-(1H-indol-4-yl)-2-methylamino-N-phenyl-acetamide XXIV (122 mg, pale yellow solid) was used without further purification for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446118B2
Source datasetuspto-grants-2008_11
ORD IDord-d7da6e8551b34a93bb747a8fa1ecbccb
Source noteuspto-grants-2008_11